chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5161354725161354726CT23GENIChomozygous141770502
5161358467161358468TA19GENIChomozygous137661532
5161358478161358479CT20GENIChomozygous141770503
5161359138161359139AC29GENIChomozygous137661533
5161359199161359200GA29GENIChomozygous141770504
5161361910161361911CA24GENICpossibly homozygous141770505
5161362859161362860TC22GENIChomozygous137661536
5161363889161363890AG35GENIChomozygous137661537
5161366228161366229GC25GENIChomozygous137661539
5161366313161366314CT25GENIChomozygous137661540
5161367376161367377CT37GENIChomozygous137661541
5161367522161367523GA27GENIChomozygous141770506
5161367640161367641TC31GENIChomozygous137661542
5161367687161367688TC35GENIChomozygous137661543
5161368979161368980CG18GENIChomozygous137661546
5161370073161370074GA26GENIChomozygous137661547
5161368780161368781AC10GENICheterozygous154251878
5161368780161368781A10GENICheterozygous403720592
5161371571161371572GA18GENIChomozygous137661548
5161371902161371903AT24GENIChomozygous141770507
5161372357161372358TC32GENIChomozygous154251881
5161372357161372358T32GENICheterozygous403164811
5161373192161373193TC30GENIChomozygous141770508
5161373767161373768CT33GENIChomozygous141770509
5161373998161373999TA35GENIChomozygous141770510
5161374295161374296CT26GENIChomozygous137661552
5161375431161375432CT20GENIChomozygous141770511
5161365172161365172A21GENIChomozygous141692086
5161359969161359970T23GENIChomozygous137351800